Canonical Allele Identifier: CA2613604001

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614741-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614741T>G , CM000673.2:g.57614741T>G	GRCh38
NC_000011.9:g.57382214T>G , CM000673.1:g.57382214T>G	GRCh37
NC_000011.8:g.57138790T>G	NCBI36
NG_009625.1:g.22188T>G , LRG_105:g.22188T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*160T>G MANE Select	ENSP00000278407.4:n.*160T>G
ENST00000528996.2:c.*560T>G	ENSP00000431226.2:n.*560T>G
ENST00000531605.2:c.*1439T>G	ENSP00000503752.1:n.*1439T>G
ENST00000619430.2:c.*160T>G	ENSP00000478572.2:n.*160T>G
ENST00000676670.1:c.*15+145T>G	ENSP00000504807.1:n.*15+145T>G
ENST00000676741.1:n.2745T>G
ENST00000677624.1:c.*1083T>G	ENSP00000503979.1:n.*1083T>G
ENST00000677625.1:c.*160T>G	ENSP00000502857.1:n.*160T>G
ENST00000677856.1:n.1916T>G
ENST00000677915.1:c.*560T>G	ENSP00000503118.1:n.*560T>G
ENST00000678533.1:c.*1072+145T>G	ENSP00000503873.1:n.*1072+145T>G
ENST00000678592.1:c.*603T>G	ENSP00000504424.1:n.*603T>G
ENST00000278407.8:c.*160T>G	ENSP00000278407.4:n.*160T>G
ENST00000340687.10:c.*160T>G	ENSP00000341861.6:n.*160T>G
ENST00000378324.6:c.*160T>G	ENSP00000367575.2:n.*160T>G
ENST00000403558.1:c.*160T>G	ENSP00000384420.1:n.*160T>G
ENST00000528996.1:c.864T>G	ENSP00000431226.1:n.864T>G
ENST00000531797.5:c.*688T>G	ENSP00000432554.1:n.*688T>G
NM_000062.2:c.*160T>G , LRG_105t1:c.*160T>G	NP_000053.2:n.*160T>G
NM_001032295.1:c.*160T>G	NP_001027466.1:n.*160T>G
NM_000062.3:c.*160T>G MANE Select	NP_000053.2:n.*160T>G
NM_001032295.2:c.*160T>G	NP_001027466.1:n.*160T>G